SRX4389464 GSM3270908 SRP153375 SRS3545809 GSM3270908 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270908 GSM3270908 GEO Accession GSM3270908 SRX4389465 GSM3270909 SRP153375 SRS3545807 GSM3270909 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270909 GSM3270909 GEO Accession GSM3270909 SRX4389466 GSM3270910 SRP153375 SRS3545804 GSM3270910 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270910 GSM3270910 GEO Accession GSM3270910 SRX4389467 GSM3270911 SRP153375 SRS3545816 GSM3270911 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270911 GSM3270911 GEO Accession GSM3270911 SRX4389468 GSM3270912 SRP153375 SRS3545806 GSM3270912 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270912 GSM3270912 GEO Accession GSM3270912 SRX4389469 GSM3270913 SRP153375 SRS3545808 GSM3270913 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270913 GSM3270913 GEO Accession GSM3270913 SRX4389470 GSM3270914 SRP153375 SRS3545815 GSM3270914 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270914 GSM3270914 GEO Accession GSM3270914 SRX4389471 GSM3270915 SRP153375 SRS3545813 GSM3270915 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270915 GSM3270915 GEO Accession GSM3270915 SRX4389472 GSM3270916 SRP153375 SRS3545814 GSM3270916 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270916 GSM3270916 GEO Accession GSM3270916 SRX4389473 GSM3270917 SRP153375 SRS3545810 GSM3270917 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270917 GSM3270917 GEO Accession GSM3270917 SRX4389474 GSM3270918 SRP153375 SRS3545811 GSM3270918 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270918 GSM3270918 GEO Accession GSM3270918 SRX4389475 GSM3270919 SRP153375 SRS3545812 GSM3270919 RNA-Seq TRANSCRIPTOMIC cDNA Brain cortices were removed, snap frozen in liquid nitrogen, homogenized and subjected to immunoprecipitation with anti-HA beads. Polyribosome-bound RNA was extracted using RNEasy Micro Plus Kit (Qiagen) and assessed for quality in BioAnalyzer 2000 (Agilent). 100 ng of RNA were used for sequencing library preparation with the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Libraries were validated in the 2100 BioAnalyzer and quantified by qPCR and fluorometric analysis (Qubit 2.0, Invitrogen). Illumina MiSeq gds 303270919 GSM3270919 GEO Accession GSM3270919